Sox-9 Polyclonal Antibody, 50ul Human Genome Knockout Libraries Mutations in this gene are

Mutations in this gene are associated with ataxia telangiectasia| an autosomal recessive disorder

it is thought that the presenilins are involved in the cleavage of the Notch receptor such that

and it may contribute to the antiviral activity of CD8 (+) T-cells

petri dishes and tubes

Sox-9 Polyclonal Antibody, 50ul Human Genome Knockout Libraries Mutations in this gene areTranscription factor SOX 9 encoded by SOX9 recognizes the sequence CCTTGAG along with other members of the HMG box class DNA binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal.